Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 1.7E-02
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 1.9E-02
CUI: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant
0 2 0 0 2 3.8E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 1.9E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous
0 2 0 0 1 1.9E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis
0 2 0 0 1 1.9E-02
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6
0 1 0 0 1 1.9E-02
CUI: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia
0 2 0 0 2 3.8E-02
CUI: C0005938
Disease: Bone Density
Bone Density
138 0 1 1.4E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria
129 0 1 1.4E-03 0 0
CUI: C0013222
Disease: Drug Use Disorders
Drug Use Disorders
121 0 1 1.5E-03 0 0
Organic Mental Disorders, Substance-Induced
115 0 1 1.5E-03 0 0
CUI: C4316881
Disease: Prescription Drug Abuse
Prescription Drug Abuse
115 0 1 1.5E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness
112 0 1 1.5E-03 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia
100 0 1 1.5E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc
98 0 1 1.5E-03 0 0
CUI: C0428568
Disease: Fasting blood glucose measurement
Fasting blood glucose measurement
96 0 1 1.5E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect
94 0 1 1.5E-03 0 0
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution
90 0 1 1.5E-03 0 0
Respiratory insufficiency due to muscle weakness
85 0 1 1.5E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 1.6E-03 0 0
CUI: C0856863
Disease: Broad-based gait
Broad-based gait
75 0 1 1.6E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia
75 0 1 1.6E-03 0 0
CUI: C1857453
Disease: Renal hypoplasia/aplasia
Renal hypoplasia/aplasia
73 0 1 1.6E-03 0 0
CUI: C1844813
Disease: Widely spaced teeth
Widely spaced teeth
71 0 1 1.6E-03 0 0